Officer (Quality Control)

Job Description of Q.C Officer

A Quality Control (QC) Officer in the pharmaceutical industry ensures that products meet quality standards and regulatory requirements throughout the manufacturing process. Their responsibilities include analysing raw materials, in-process samples, and finished products, maintaining instruments, and ensuring adherence to cGMP and other relevant guidelines. They also document findings, investigate deviations, and support continuous improvement efforts.

Key Responsibilities:

· Sampling and Analysis:

· Collecting and testing samples of raw materials, in-process materials, and finished products.

· Performing various analytical techniques, including wet chemistry and instrumental analysis.

· Analysing stability samples and preparing stability trend reports.

· Status labelling of quality control Instruments, Chemical & Glassware.

· Disposal of balance samples after completion of analysis and its documentation.

· Instrument Maintenance and Calibration:

· Maintaining and calibrating QC instruments, including HPLC, spectrophotometers, etc.

· Documentation and Record Keeping:

· Maintaining detailed records of analysis, including instrument logbooks, method validations, and SOPs.

· Preparing and reviewing stability protocols and reports.

· Preparation of certificates of analysis (COA)

· Method Validation and Transfer:

· Participating in method validation and transfer activities.

· Deviation Reporting and CAPA:

· Reporting and investigating deviations from established procedures and specifications.

· Participating in the development and implementation of corrective and preventative actions (CAPAs).

· Compliance and Auditing:

· Ensuring compliance with cGMP, ICH, USFDA, ISO, and other relevant guidelines.

· Providing documentation to auditors and assisting with audit activities.

· Continuous Improvement:

· Identifying areas for improvement in QC processes and procedures.

· Supporting the implementation of new technologies and methods.

Qualifications:

· Bachelor's degree in chemistry, pharmacy, M.Sc. (Chemistry) or a related field.

· Experience in pharmaceutical QC, preferably with a focus on analytical chemistry.

· Knowledge of cGMP, ICH, USFDA, and other relevant guidelines.

· Proficiency in various analytical techniques and instrumentation.

· Strong analytical, problem-solving, and communication skills.

Job Types: Full-time, Permanent

Pay: ₹11,284.71 - ₹20,000.00 per month

Benefits:

• Paid sick time
• Provident Fund

Work Location: In person

Application Deadline: 15/05/2025
Expected Start Date: 01/08/2025